Claims for Patent: 4,628,051

Summary for Patent: 4,628,051

Title:	Triphasic oral contraceptive
Abstract:	A method of contraception in which an estrogen and a progestogen are administered daily in a three phase sequence for 21 days is disclosed. In the first phase a combination of an estrogen and a progestogen in a low but contraceptively effective daily dosage corresponding in estrogenic activity to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.065-0.75 mg of norethindrone is administered for 5-8 days; followed by the administering of the same dosage of estrogen and a progestogen corresponding in progestogenic activity to 0.25-1.0 mg of norethindrone for 7-11 days; followed by the administering of the same dosage of estrogen and a progestogen corresponding in progestogenic activity to 0.35-2.0 mg of norethindrone for 3-7 days; followed by 6-8 days without administering either an estrogen or a progestogen.
Inventor(s):	Pasquale; Samuel A. (Basking Ridge, NJ)
Assignee:	Ortho Pharmaceutical Corporation (Raritan, NJ)
Application Number:	06/743,344
Patent Claims:	1. A method of contraception which comprises administering for 21 successive days to a female of childbearing age a combination of an estrogen and a progestogen in a low but contraceptively effective daily dosage corresponding in estrogenic activity to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.065-0.75 mg of norethindrone for 5-8 days; for the next 7-11 days an estrogen daily dosage equal to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.250-1.0 mg of norethindrone; and for the next 3-7 days an estrogen daily dosage equal to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity 0.35-2.0 mg of norethindrone; followed by 6-8 days without estrogen and progestogen administration, provided that the estrogen daily dosage is the same for each period. 2. The method of claim 1 wherein the estrogen and progestogen are administered orally and the period specified in each phase is seven days. 3. The method of claim 2 wherein the estrogen and progestogen are administered in admixture. 4. The method of claim 1 wherein the progestogen is selected from the group consisting of D-norgestrel, .DELTA..sup.15 levonorgestrel, .DELTA..sup.15 levonorgestrel acetate, .DELTA..sup.15 levonorgestrel acetate oxime, norethindrone, progesterone and D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime. 5. The method of claim 1 wherein the estrogen is selected from the group consisting of 17.alpha.-ethinylestradiol, mestranol, estrone, estrone sulfate piperazine salt, estradiol and estriol. 6. The method of claim 3 wherein the estrogen is 17.alpha.-ethinylestradiol and the progestogen is norethindrone. 7. The method of claim 3 wherein the estrogen is 17.alpha.-ethinylestradiol 3-methyl ether and the progestogen is norethindrone. 8. The method of claim 1 wherein the estrogen is 17.alpha.-ethinylestradiol and the progestogen is D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime. 9. The method of claim 1 wherein the estrogen is 17.alpha.-ethinylestradiol 3-methyl ether and the progestogen is D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime. 10. The method of claim 6 wherein the estrogen daily dosage is 0.035 mg for each 7 day period and the progestogen daily dosage is 0.5 mg for the first 7 days, 0.75 mg for the second 7 days and 1.0 mg for the third 7 days. 11. The contraception method of claim 1 which comprises administering for 21 successive days to a female of childbearing age a combination of 17.alpha.-ethinylestradiol and norethindrone in a contraceptively effective daily dosage corresponding to 0.035 mg of 17.alpha.-ethinylestradiol and 0.50 mg of norethindrone for 7 daysa daily dosage equal to 0.035 mg of 17.alpha.-ethinylestradiol and 0.75 mg of norethindrone; and for the next 7 days a daily dosage equal to 0.035 mg of 17.alpha.-ethinylestradiol and 1.0 mg of norethindrone; followed by 7 days without estrogen and progestogen administration. 12. The contraception method of claim 1 which comprises administering for 21 successive days to a female of childbearing age a combination of 17.alpha.-ethinylestradiol and D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime in a contraceptively effective daily dosage corresponding to 0.035 mg of 17.alpha.-ethinylestradiol and 0.180 mg of D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime for 7 days; for the next 7 days a daily dosage equal to 0.035 mg of 17.alpha.-ethinylestradiol and 0.215 mg of D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime; and for the next 7 days a daily dosage equal to 0.035 mg of 17.alpha.-ethinylestradiol and 0.250 mg of D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime; followed by 7 days without estrogen and progestogen administration. 13. A triphasic oral contraceptive unit consisting of 21 separate dosage units, adapted for successive daily oral administration comprising: 7 dosage units containing, in admixture with a pharmaceutically acceptable carrier, a combination of an estrogen and a progestogen at contraceptively effective dosages corresponding in activity to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.065-0.75 mg of norethindrone as the first phase; followed by 7 dosage units containing in admixture with a pharmaceutically acceptable carrier, a combination of an estrogen at a contraceptively effective dosage corresponding in activity to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.25-1.0 mg of norethindrone as the second phase; followed by 7 dosage units containing in admixture with a pharmaceutically acceptable carrier, a combination of an estrogen at a contraceptively effective dosage corresponding to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.35-2.0 mg of norethindrone as the third phase, and optionally containing 7 dosage units free of estrogen and progestogen; provided that the estrogen daily dosage is the same in all three phases. 14. The unit according to claim 13 wherein the dosage units are in the form of tablets. 15. The unit according to claim 13 wherein the estrogen is selected from the group consisting of 17.alpha.-ethinylestradiol, mestranol, estrone, estrone sulfate, estrone sulfate piperazine salt, estradiol and estriol. 16. The unit according to claim 14 wherein the estrogen is 17.alpha.-ethinylestradiol. 17. The unit according to claim 13 wherein the estrogen is 17.alpha.-ethinylestradiol 3-methyl ether. 18. The unit according to claim 13 wherein the progestogen is selected from the group consisting of D-norgestrel, .DELTA..sup.15 levonorgestrel, .DELTA..sup.15 levonorgestrel acetate, .DELTA..sup.15 levonorgestrel acetate oxime, norethindrone, progesterone and D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime. 19. The unit according to claim 18 wherein the progestogen is norethindrone. 20. The unit according to claim 18 wherein the progestogen is D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime. 21. The unit according to claim 13 wherein the estrogen is 17.alpha.-ethinylestradiol 3-methyl ether and the progestogen is norethindrone. 22. The unit according to claim 13 wherein the estrogen is 17.alpha.-ethinylestradiol 3-methyl ether and the progestogen is D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime. 23. A composition according to claim 13 wherein the estrogen daily dosage in all three phases is equivalent to 0.035 mg of 17.alpha.-ethinylestradiol; and the progestogen daily dosage is equivalent to 0.50 mg of norethindrone in the first phase, 0.75 mg of norethindrone in the second phase and 1.0 mg of norethindrione in the third phase. 24. A composition according to claim 13 wherein the estrogen daily dosage in all three phases is equivalent to 0.035 mg of 17.alpha.-ethinylestradiol; and the progestogen daily dosage is equivalent to 0.180 mg of D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime in the first phase, 0.215 mg of D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime in the second phase and 0.250 mg of D-17.beta.-acetoxy-13.beta.-ethyl-17.alpha.-ethinyl-gon-4-en-3-one oxime in the third phase. 25. A triphasic oral contraceptive unit consisting of 21 separate dosage units, adapted for successive daily oral administration comprising: 5-8 dosage units containing, in admixture with a pharmaceutically acceptable carrier, a combination of an estrogen and a progestogen at contraceptively effective dosages corresponding in activity to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.065-0.75 mg of norethindrone as the first phase; followed by 7-11 dosage units containing in admixture with a pharmaceutically acceptable carrier, a combination of an estrogen at a contraceptively effective dosage corresponding in activity to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.25-1.0 mg of norethindrone as the second phase; followed by 3-7 dosage units containing in admixture with a pharmaceutically acceptable carrier, a combination of an estrogen at a contraceptively effective dosage corresponding to 0.02-0.05 mg of 17.alpha.-ethinylestradiol and in progestogenic activity to 0.35-2.0 mg of norethindrone as the third phase, and optionally containing 6-8 dosage units free of estrogen and progestogen; provided that the estrogen daily dosage is the same in all three phases.